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配水系统中双酚A的转化:中试规模研究。

Transformation of bisphenol A in water distribution systems: a pilot-scale study.

作者信息

Li Cong, Wang Zilong, Yang Y Jeffrey, Liu Jingqing, Mao Xinwei, Zhang Yan

机构信息

College of Civil Engineering and Architecture, Zhejiang University, Hangzhou, China.

U.S. EPA, National Risk Management Research Laboratory, Cincinnati, USA.

出版信息

Chemosphere. 2015 Apr;125:86-93. doi: 10.1016/j.chemosphere.2014.11.047. Epub 2014 Dec 27.

Abstract

Halogenations of bisphenol A (BPA) in a pilot-scale water distribution system (WDS) of a cement-lined ductile cast iron pipe were investigated. The water in the pilot-scale WDS was chlorinated with a free chlorine concentration of 0.7 mg L(-1) using sodium hypochlorite, and with an initial BPA concentration of 100 μg L(-1) was spiked in the WDS. Halogenated compounds in the BPA experiments were identified using EI/GC/MS and GC. Several BPA congeners, including 2-chlorobisphenol A (MCBPA), dichlorobisphenol A (D2-CBPA), 2,2',6-trichlorobisphenol A (T3CBPA), 2,2',6,6'-tetrachlorobisphenol A (T4CBPA), 2-bromobisphenol A (MBBPA), and bromochlorobisphenol A (MBMCBPA) were found. Moreover, further halogenation yielded other reaction intermediates, including 2,4,6-trichlorophenol (T3CP), dichlorobisphenol A, bromodichlorophenol, and dibromochlorophenol. After halogenation for 120min, most of the abovementioned reaction intermediates disappeared and were replaced by trihalomethanes (THMs). Based on these experimental findings, the halogenation process of BPA oxidation in a WDS includes three stages: (1) halogenation on the aromatic ring; (2) chlorine or bromine substitution followed by cleavage of the α-C bond on the isopropyl moiety with a positive partial charge and a β'-C bond on the benzene moiety with a negative partial charge; and (3) THMs and a minor HAA formation from phenolic intermediates through the benzene ring opening with a chlorine and bromine substitution of the hydrogen on the carbon atoms. The oxidation mechanisms of the entire transformation from BPA to THM/HAA in the WDS were proposed.

摘要

在一个内衬水泥的球墨铸铁管中试规模配水系统(WDS)中,对双酚A(BPA)的卤化反应进行了研究。中试规模WDS中的水使用次氯酸钠进行氯化处理,使游离氯浓度达到0.7 mg L⁻¹,并向WDS中加入初始浓度为100 μg L⁻¹的双酚A。在双酚A实验中,使用电子轰击电离/气相色谱/质谱联用仪(EI/GC/MS)和气相色谱(GC)鉴定卤化化合物。发现了几种双酚A同系物,包括2 - 氯双酚A(MCBPA)、二氯双酚A(D2 - CBPA)、2,2',6 - 三氯双酚A(T3CBPA)、2,2',6,6' - 四氯双酚A(T4CBPA)、2 - 溴双酚A(MBBPA)和溴氯双酚A(MBMCBPA)。此外,进一步卤化产生了其他反应中间体,包括2,4,6 - 三氯苯酚(T3CP)、二氯双酚A、溴二氯苯酚和二溴氯苯酚。卤化120分钟后,上述大多数反应中间体消失,并被三卤甲烷(THMs)取代。基于这些实验结果,WDS中双酚A氧化的卤化过程包括三个阶段:(1)芳环上的卤化;(2)氯或溴取代,随后异丙基部分带正部分电荷的α - C键和苯部分带负部分电荷的β' - C键断裂;(3)酚类中间体通过苯环开环,碳原子上的氢被氯和溴取代,形成THMs和少量卤乙酸(HAA)。提出了WDS中双酚A向THM/HAA完全转化的氧化机理。

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